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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1401976생성일: 2026년 10월 26일

Sodium Sulfate → Tert-butyl 4-(5-chloro-2-methoxyphenyl)-4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/1401976

반응식

참여 물질

역할이름HCID투입량
반응물Sodium SulfateHCID 24436—
반응물Sodium BisulfateHCID 516919—
반응물2-Bromo-4-chloroanisoleHCID 521935—
반응물tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Tert-butyl 4-(5-chloro-2-methoxyphenyl)-4-hydroxypiperidine-1-carboxylateHCID 5877248039%

반응 조건

온도-70 °C

반응 단계

To a stirred solution of 2-bromo-4-chloroanisole (164 g, 0.74 mol) in tetrahydrofuran (1 L), cooled at −70° C. and under an atmosphere of argon, was added butyl lithium (2.7 M in heptane, 280 ml) over a period of 1 hour. The mixture was stirred for 30 minutes, maintaining the temperature at −70° C., before the addition of N-boc-4-piperidone (145 g, 0.73 mol) in tetrahydrofuran (250 ml) over a period of 1 hour. The reaction temperature was warmed to −40° C. over 2 hours before the addition of sodium hydrogen sulphate (5M aqueous, 160 ml), sodium sulphate (300 g) and hexane (500 ml). The mixture was stirred for 10 hours. The organic layer was decanted, filtered through silica gel (300 g, 63/100 μm) washing with ethyl acetate:hexane (4:6, by volume, 2×400 ml). The filtrate was evaporated in vacuo and the residue recrystallized from ethyl acetate:hexane to afford the title compound as white crystals, 100 g, 39% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08907101B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-b547530a686e4e11ad75cb3f5b5eb618
출처 메모uspto-grants-2014_12